Canonical Allele Identifier: CA2466723598

Gene: G6PD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154533037G= , CM000685.2:g.154533037G=	GRCh38
NC_000023.10:g.153761252G= , CM000685.1:g.153761252G=	GRCh37
NC_000023.9:g.153414446G=	NCBI36
NG_009015.2:g.19536C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.956C=	ENSP00000377194.2:p.Thr319=
ENST00000439227.6:c.959C=	ENSP00000395599.2:p.Thr320=
ENST00000696420.1:c.956C=	ENSP00000512615.1:p.Thr319=
ENST00000696421.1:c.956C=	ENSP00000512616.1:p.Thr319=
ENST00000696422.1:c.819C=
ENST00000696423.1:c.822C=
ENST00000696424.1:c.808C=	ENSP00000512619.1:n.808C=
ENST00000696425.1:c.865-235C=	ENSP00000512620.1:n.865-235C=
ENST00000696426.1:c.*416C=	ENSP00000512621.1:n.*416C=
ENST00000696427.1:c.963C=	ENSP00000512622.1:p.His321=
ENST00000696428.1:c.*798C=	ENSP00000512623.1:n.*798C=
ENST00000696429.1:c.956C=	ENSP00000512624.1:p.Thr319=
ENST00000696430.1:c.956C=	ENSP00000512625.1:p.Thr319=
ENST00000393562.10:c.956C= MANE Select	ENSP00000377192.3:p.Thr319=
ENST00000369620.6:c.1094C=	ENSP00000358633.2:p.Thr365=
ENST00000393562.6:c.1046C=	ENSP00000377192.2:p.Thr349=
ENST00000393564.6:c.956C=	ENSP00000377194.2:p.Thr319=
ENST00000439227.5:c.959C=	ENSP00000395599.1:p.Thr320=
ENST00000440967.5:c.959C=	ENSP00000400648.1:p.Thr320=
ENST00000490651.1:n.38C=
ENST00000621232.4:c.956C=	ENSP00000483686.1:p.Thr319=
NM_000402.4:c.1046C=	NP_000393.4:p.Thr349=
NM_001042351.2:c.956C=	NP_001035810.1:p.Thr319=
XM_005274657.2:c.1049C=	XP_005274714.1:p.Thr350=
XM_005274658.2:c.959C=	XP_005274715.1:p.Thr320=
XM_011531132.1:c.958-235C=	XP_011529434.1:n.958-235C=
NM_001360016.2:c.956C= MANE Select	NP_001346945.1:p.Thr319=
NM_001042351.3:c.956C=	NP_001035810.1:p.Thr319=